7 results
·
28ms
·
Sources: EU EUDAMED, US FDA
SONIBRUSH
FDA 510(k)
FDA Class 1
·Dental
LP Low Profile
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746090820·DB BKT LP LR CUSP 022 T=0 A+5 R=0
AUTO SUTURE ENDOSCOPIC KNOT PUSHER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
TITAN GEL
FDA 510(k)
FDA Class 2
·Immunology
MEDTRONIC.SIGMA
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code NVZ·January 30, 2013
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 3, 2014
REPAIR CORE RECIP SAW
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS KALAMAZOO·Product code DZJ·December 6, 2010